Canonical Allele Identifier: CA505749492
Gene: ODAD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11533446C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11422778C>G , CM000681.2:g.11422778C>G GRCh38
NC_000019.9:g.11533446C>G , CM000681.1:g.11533446C>G GRCh37
NC_000019.8:g.11394446C>G NCBI36
NG_041777.1:g.18005G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356392.9:c.1200G>C MANE Select ENSP00000348757.3:p.Val400=
ENST00000356392.8:c.1200G>C ENSP00000348757.3:p.Val400=
ENST00000586836.5:c.627G>C ENSP00000467429.1:p.Val209=
ENST00000591179.5:c.1020G>C ENSP00000466800.1:p.Val340=
ENST00000591345.5:c.*1119G>C ENSP00000467313.1:n.*1119G>C
NM_001302453.1:c.1038G>C NP_001289382.1:p.Val346=
NM_001302454.1:c.1020G>C NP_001289383.1:p.Val340=
NM_145045.4:c.1200G>C NP_659482.3:p.Val400=
XM_017026241.1:c.*94G>C XP_016881730.1:n.*94G>C
NM_145045.5:c.1200G>C MANE Select NP_659482.3:p.Val400=
NM_001302454.2:c.1020G>C NP_001289383.1:p.Val340=